16 X 125 MM TEST TUBE, CATALOG #01-241— 510(k) K930388

Name: FDA 510(k) clearance K930388
Creator: U.S. Food and Drug Administration
Published: 1993-03-23

Substantially Equivalent

Proteins Intl., Inc.

FDA 510(k) clearance K930388 for 16 X 125 MM TEST TUBE, CATALOG #01-241, Substantially Equivalent on 1993-03-23. Applicant: Proteins Intl., Inc.. Device class: 1.

Clearance details

Applicant: Proteins Intl., Inc.
Product code: Code KIR
Device class: Class 1
Regulation: 21 CFR 864.2280
Advisory panel: Hematology
Date received: 1993-01-26
Decision date: 1993-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester Hills, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIR

view all

K973209 — FRESH CELLS VERO1997-09-25
K973210 — FRESH CELLS NCI H2921997-09-25
K973211 — FRESH CELLS MV1LU1997-09-25
K973212 — FRESH CELLS WI-381997-09-25
K973213 — FRESH CELLS LLC-MK21997-09-25

More clearances from Proteins Intl., Inc.

view all

K961755 — CYTOQUANT CHLAMYDIA TRANSPORT MEDIUM1996-05-17
K961756 — CYTOQUANT VIRAL TRANSPORT MEDIUM1996-05-17
K930390 — 25 CM2, 75 CM2, 125 CM2 FLASK, CATALOG #03-2911993-03-24
K930391 — 25 CM2, 75 CM2, 150 CM2 FLASK, CATALOG #03-2611993-03-24
K930392 — 16 X 125 MM TEST TUBE, CATALOG #01-1111993-03-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.